Unique variants in gene RXFP2

Information The variants shown are described using the NM_130806.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Reported     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
?/. 1 - c.497T>C r.(?) p.(Ile166Thr) - VUS g.32340164T>C - RXFP2(NM_130806.4):c.497T>C (p.I166T) - RXFP2_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
-?/. 1 - c.1594C>G r.(?) p.(Arg532Gly) - likely benign g.32367033C>G g.31792896C>G RXFP2(NM_001166058.1):c.1522C>G (p.(Arg508Gly)) - RXFP2_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
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